An injection device is described including a detection unit that includes an electrode that detects electrical characteristics of a biological tissue, a follow-up mechanism that follows motions of the biological tissue, and a puncture unit capable of puncturing the biological tissue. The injection device is configured to administer a predetermined substance to the biological tissue through a hollow portion defined in the puncture unit. A position of the puncture unit is specified based on a position of the electrode. The follow-up mechanism includes a spiral portion spirally extending around the puncture unit, and being stretchable and compressible along an extending direction of the puncture unit. Electrodes are disposed on an annular distal-end projected plane of the spiral portion, as seen from a distal end side of the puncture unit, along a circumferential direction of the puncture unit.

The present disclosure describes a personal vaporizer which can detect whether or not a cartridge of the personal vaporizer has been breached. The cartridge includes a conductive shell. The conductive shell can include two or more conductors which are electrically isolated from each-other. Prior to operation, the personal vaporizer can use the two or more conductors to assess whether or not an outer shell of the cartridge has been breached. In some implementations, if it is determined that the cartridge has been breached, the personal vaporizer can shut down, or otherwise fail to operate normally.

A droplet delivery device and related methods for delivering precise and repeatable dosages to a subject for pulmonary use is disclosed. The droplet delivery device includes a housing, a reservoir, and ejector mechanism, and at least one differential pressure sensor. The droplet delivery device is automatically breath actuated by the user when the differential pressure sensor senses a predetermined pressure change within housing. The droplet delivery device is then actuated to generate a stream of droplets having an average ejected droplet diameter within the respirable size range, e.g, less than about 5 μm, so as to target the pulmonary system of the user.

An apparatus for monitoring EMG signals of a patient's laryngeal muscles includes an endotracheal tube having an exterior surface and a first location configured to be positioned at the patient's vocal folds. A first electrode is formed on the exterior surface of the endotracheal tube substantially below the first location to receive EMG signals primarily from below the vocal folds. A second electrode is formed on the exterior surface of the endotracheal tube substantially above the first location to receive EMG signals primarily from above the vocal folds. The first and second electrodes are configured to receive the EMG signals from the laryngeal muscles when the endotracheal tube is placed in a trachea of the patient.

A fluid flow sensing and bubble detecting apparatus, comprising:—housing provided with a cavity configured to receive a tube through which conductive fluid flows;—a fluid flow sensing and bubble detecting electrical sensor assembly supported by the housing and configured to sense the flow of the fluid flowing through the tube and to detect bubbles in the fluid; and—an electrically grounded Electro-Magnetic Interference (EMI) shielding arranged between at least a part of the sensor assembly and the cavity such that the EMI shielding protects the sensor assembly from unwanted EMI emanating from a tube received within the cavity, which might otherwise cause the fluid flow sensing and bubble detecting apparatus to generate false bubble detection signals.

In an exemplary embodiment, a drug delivery device is configured for Body Channel Communication (BCC). The drug delivery device may include a conductive element embedded in an adhesive patch that secures the drug delivery device to the user. This conductive element acts as a coupler to the body of the user. Another conductive element may also be provided at a face of the housing. This conductive element acts as the other end of the coupler formed with the conductive coil in the adhesive patch. The conductive coil in the adhesive patch conforms well to the user's skin surface and thus facilitates a good quality coupling with the user.

Infusion pump control unit keypad assemblies are provided, and include a cover assembly having an outer surface and an inner surface and a perimeter gasket disposed within a raised perimeter on the outer surface of the cover assembly. A lens and a circuit assembly are coupled to the outer surface of the cover assembly. A switch assembly is coupled to the circuit assembly, a shield assembly is coupled to the switch assembly, a light assembly is coupled to the shield assembly and an overlay assembly is coupled to the light assembly. Methods of making infusion pump control unit keypad assemblies are also provided.

The invention relates to a valveless spacer device for a metered dose inhaler (MDI), the spacer device comprising a body having an inlet and an outlet opposed from the inlet, a demountable, flexible bag attached to the body, the bag and body together defining a chamber, such that the inlet and outlet are in fluid flow communication with an interior of the chamber, wherein the inlet is configured to be connected to an MDI containing a drug to be inhaled and wherein the flexible bag, following actuation of the MDI, serves as a reservoir allowing for the formation of a cloud or mist of the drug therewithin which is then ready for inhalation, the flexible bag being configured to be at least partially deflatable and at least partially inflatable commensurate with a single breath and/or rebreathing.

The invention relates to a connecting piece for establishing a fluid connection between fluid-conducting lines for installation in a cut-out in a housing part of a medical device, in particular a dialysis unit. Furthermore, the invention relates to a medical device, in particular a dialysis unit, comprising a housing that comprises a housing part having a cut-out into which a connecting piece of this type is inserted. The connecting piece 13 according to the invention comprises a tubular body 18 that is made of an electrically conductive material and can be inserted into the cut-out 23 in the housing part 1A, the end pieces 19, 20 of which body are designed for the attachment of the fluid-conducting lines. The connecting piece 13 is distinguished by a terminal part 16 for attaching an electrical protective conductor or equipotential bonding system, the terminal part 16 being electrically conductively connectable or connected to the tubular body 18. The terminal part 16 allows an electrical connection cable 17 to be directly attached to a protective conductor 15 (PE conductor).

A modular, semi-disposable patch pump for conducting a medical therapy includes a pump unit releasably connected to a reservoir unit by means of a bayonet connection; and a housing design for supporting both reliability and ease of use of said connection.